期刊
ACS CATALYSIS
卷 12, 期 15, 页码 8936-8975出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c02629
关键词
N-2 fixation; electrochemical; NH3 synthesis; reaction mechanism; catalyst design; computational catalysis
资金
- Westlake University
- Zhejiang Province
This review summarizes the recent research progress in electrochemical nitrogen reduction reaction (eNRR) in ammonia synthesis, highlighting the current challenges and future opportunities, and pointing out the need for further efforts in mechanistic understanding and catalyst design.
Large-scale ammonia synthesis via the electrochemical nitrogen reduction reaction (eNRR) under mild reaction conditions represents a green prospect for agriculture, industry, and energy. This bioinspired and carbon-free reaction has been proposed as an ideal alternative to the Haber-Bosch process. However, the yield and selectivity of the current eNRR have not met the requirements for industrialization. Mechanistic understanding and catalysts' design are still long-term pursuits in this field, where theoretical simulations will have significant contributions. In this Review, we will start with the natural N-2 fixation enzymes, the nitrogenases, followed by a summary of the key experimental eNRR performances on hundreds of recently reported catalysts, and we analyze the general trend and challenges before eNRR can significantly impact the ammonia industry. Then, we will systematically review the recent progress and contributions of computational studies in understanding the reaction mechanism and rational catalyst design for eNRR. The fundamental principles, reaction mechanisms, crucial theoretical criteria, modeling methods, and computationally predicted catalysts for eNRR are systematically summarized and discussed. Finally, we outline the current challenges and future opportunities for experimental and computational studies of electrochemical N-2 reduction.
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